Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 243

1.

Molecular genetic basis of Gilbert's syndrome.

Burchell B, Hume R.

J Gastroenterol Hepatol. 1999 Oct;14(10):960-6. Review.

PMID:
10530490
2.
3.

Gilbert's syndrome is a contributory factor in prolonged unconjugated hyperbilirubinemia of the newborn.

Monaghan G, McLellan A, McGeehan A, Li Volti S, Mollica F, Salemi I, Din Z, Cassidy A, Hume R, Burchell B.

J Pediatr. 1999 Apr;134(4):441-6.

PMID:
10190918
4.

TATA-box mutant in the promoter of the uridine diphosphate glucuronosyltransferase gene in Italian patients with Gilbert's syndrome.

Sampietro M, Lupica L, Perrero L, Romano R, Molteni V, Fiorelli G.

Ital J Gastroenterol Hepatol. 1998 Apr;30(2):194-8.

PMID:
9675658
5.

The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome.

Bosma PJ, Chowdhury JR, Bakker C, Gantla S, de Boer A, Oostra BA, Lindhout D, Tytgat GN, Jansen PL, Oude Elferink RP, et al.

N Engl J Med. 1995 Nov 2;333(18):1171-5.

7.

Restriction fragment length polymorphism effectively identifies exon 1 mutation of UGT1A1 gene in patients with Gilbert's Syndrome.

Shiu TY, Huang HH, Lin HH, Shih YL, Chu HC, Chang WK, Hsieh TY.

Liver Int. 2015 Aug;35(8):2050-6. doi: 10.1111/liv.12785. Epub 2015 Feb 6.

PMID:
25611851
8.

[A study of polymorphism in UDP-glucuronosyltransferase 1 (UGT-1A1) promoter gene in Korean patients with Gilbert's syndrome].

Kim YH, Yeon JE, Jung GM, Kim HJ, Kim JS, Byun KS, Bak YT, Lee CH.

Taehan Kan Hakhoe Chi. 2002 Jun;8(2):132-8. Korean.

9.

Genetic variation in bilirubin UPD-glucuronosyltransferase gene promoter and Gilbert's syndrome.

Monaghan G, Ryan M, Seddon R, Hume R, Burchell B.

Lancet. 1996 Mar 2;347(9001):578-81.

PMID:
8596320
10.

Rapid molecular diagnosis of the Gilbert's syndrome-associated exon 1 mutation within the UGT1A1 gene.

Hsieh TY, Shiu TY, Chu NF, Chao TY, Chu HC, Chang WK, Chao YC, Huang HH.

Genet Mol Res. 2014 Jan 28;13(1):670-9. doi: 10.4238/2014.January.28.12.

11.

Correlation of mutational analysis to clinical features in Taiwanese patients with Gilbert's syndrome.

Hsieh SY, Wu YH, Lin DY, Chu CM, Wu M, Liaw YF.

Am J Gastroenterol. 2001 Apr;96(4):1188-93.

PMID:
11316168
12.

Development of icterus gravis in a preterm infant with G71R UGT1A1 polymorphism.

Kaga A, Ohkubo Y, Watanabe Y, Saito S, Matsuki T, Usuda H, Kanda S, Suzuki Y, Tanabu M, Kure S.

BMC Res Notes. 2013 Feb 6;6:51. doi: 10.1186/1756-0500-6-51.

13.

The combination of new missense mutation with [A(TA)7TAA] dinucleotide repeat in UGT1A1 gene promoter causes Gilbert's syndrome.

D'Angelo R, Rinaldi C, Donato L, Nicocia G, Sidoti A.

Ann Clin Lab Sci. 2015 Spring;45(2):202-5.

PMID:
25887876
14.

Donor liver uridine diphosphate (UDP)-glucuronosyltransferase-1A1 deficiency causing Gilbert's syndrome in liver transplant recipients.

Te HS, Schiano TD, Das S, Kuan SF, DasGupta K, Conjeevaram HS, Baker AL.

Transplantation. 2000 May 15;69(9):1882-6.

PMID:
10830226
15.

Correlation of UGT1A1 TATA-box polymorphism and jaundice in breastfed newborns-early presentation of Gilbert's syndrome.

Žaja O, Tiljak MK, Štefanović M, Tumbri J, Jurčić Z.

J Matern Fetal Neonatal Med. 2014 May;27(8):844-50. doi: 10.3109/14767058.2013.837879. Epub 2013 Sep 19.

PMID:
23981182
16.

Analyses of polymorphism for UGT1*1 exon 1 promoter in neonates with pathologic and prolonged jaundice.

Ulgenalp A, Duman N, Schaefer FV, Whetsell L, Bora E, Gülcan H, Kumral A, Oren H, Giray O, Erçal D, Ozkan H.

Biol Neonate. 2003;83(4):258-62.

PMID:
12743455
17.

Genetic variation underlying common hereditary hyperbilirubinaemia (Gilbert's syndrome) and respiratory health in the 1946 British birth cohort.

Horsfall LJ, Hardy R, Wong A, Kuh D, Swallow DM.

J Hepatol. 2014 Dec;61(6):1344-51. doi: 10.1016/j.jhep.2014.07.028. Epub 2014 Jul 31.

18.

Genetic polymorphisms of bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese patients with Crigler-Najjar syndrome or Gilbert's syndrome as well as in healthy Japanese subjects.

Takeuchi K, Kobayashi Y, Tamaki S, Ishihara T, Maruo Y, Araki J, Mifuji R, Itani T, Kuroda M, Sato H, Kaito M, Adachi Y.

J Gastroenterol Hepatol. 2004 Sep;19(9):1023-8.

PMID:
15304120
19.

The expression of uridine diphosphate glucuronosyltransferase gene is a major determinant of bilirubin level in heterozygous beta-thalassaemia and in glucose-6-phosphate dehydrogenase deficiency.

Sampietro M, Lupica L, Perrero L, Comino A, Martinez di Montemuros F, Cappellini MD, Fiorelli G.

Br J Haematol. 1997 Nov;99(2):437-9.

PMID:
9375769
20.

Supplemental Content

Support Center